Tag | Content |
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EnhancerAtlas ID | HS041-01058 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:43997340-43999860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:43998859-43998877 | CCTCCCTTTCTTCCTTCT | - | 6.52 | EWSR1-FLI1 | MA0149.1 | chr1:43998851-43998869 | CCTTCCTTCCTCCCTTTC | - | 8.52 | EWSR1-FLI1 | MA0149.1 | chr1:43998855-43998873 | CCTTCCTCCCTTTCTTCC | - | 8.64 | EWSR1-FLI1 | MA0149.1 | chr1:43998843-43998861 | AATTCCTTCCTTCCTTCC | - | 8.86 | EWSR1-FLI1 | MA0149.1 | chr1:43998847-43998865 | CCTTCCTTCCTTCCTCCC | - | 9.47 | RREB1 | MA0073.1 | chr1:43998539-43998559 | ACCCCCTCCACCCCCACACA | + | 6.23 | RREB1 | MA0073.1 | chr1:43998957-43998977 | GAGGAGGGGGTGGTTGGGTG | - | 6.39 | ZNF263 | MA0528.1 | chr1:43998846-43998867 | TCCTTCCTTCCTTCCTCCCTT | - | 6.28 | ZNF263 | MA0528.1 | chr1:43998858-43998879 | TCCTCCCTTTCTTCCTTCTTC | - | 7.16 | ZNF263 | MA0528.1 | chr1:43998855-43998876 | CCTTCCTCCCTTTCTTCCTTC | - | 7.63 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:43995107-43998898 | Adipose_Nuclei | SE_00616 | chr1:43998907-44001249 | Adipose_Nuclei | SE_04240 | chr1:43997230-43998647 | Brain_Anterior_Caudate | SE_05040 | chr1:43996981-44000130 | Brain_Cingulate_Gyrus | SE_05962 | chr1:43995415-44000121 | Brain_Hippocampus_Middle | SE_07193 | chr1:43995683-43999544 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:43997264-44000544 | Brain_Inferior_Temporal_Lobe | SE_23218 | chr1:43996011-43999623 | Colon_Crypt_1 | SE_23829 | chr1:43996144-43998350 | Colon_Crypt_2 | SE_23829 | chr1:43999234-43999589 | Colon_Crypt_2 | SE_24870 | chr1:43996197-43999448 | Colon_Crypt_3 | SE_26649 | chr1:43995723-44004223 | Esophagus | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | SE_28595 | chr1:43995607-44004348 | Fetal_Intestine_Large | SE_31538 | chr1:43995971-44000533 | Gastric | SE_41575 | chr1:43998407-43998733 | LNCaP | SE_41575 | chr1:43998859-44001617 | LNCaP | SE_47657 | chr1:43998383-43998667 | Pancreas | SE_47657 | chr1:43999225-43999586 | Pancreas | SE_50363 | chr1:43995694-44004359 | Sigmoid_Colon | SE_52524 | chr1:43995689-44000339 | Small_Intestine | SE_56987 | chr1:43995814-43998375 | VACO_400 | SE_65452 | chr1:43996948-43999005 | Pancreatic_islets | SE_65452 | chr1:43999008-43999882 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 43997843 | 43998152 | chr1 | 43999309 | 43999502 |
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Enhancer Sequence | CCCCCCACCC CCTTCGTTCG CGAGCACGGG ATGGGGAGGG GCCGAACGGG CTGTACCCGC 60 CCCCAACCGG GTGCAACGCC CTGGAGGCCC TGGAGCGACC TGTCCCGTGA GGACGTGGCC 120 ACTCGGACCC TCTCCGAAAG TTCACTCAGT GGCCGCCCCG CGTCCCGTCC CGTCCCGTCC 180 CGGCTCCCCA TCGCCGTGCC GGCGTCTCTG TCTCGGCTGC TTTCTGTTTT CCTCGGCGTC 240 TCTGCCTCCC CGTGTCAGTG CCTCCCAATC TCACGCCCCT GCAATCCCAG GGTCTCTCCA 300 GCTGTCTCCA TTCTTTTTCC CCAGGTCACT CTGTTCTTTC TCCCCAGGTC TCTCGATTCT 360 GTCTCCCTGG GTCGTCTTGT TCCCTGTCCC TGAGTCTGTT CTCTCCGCTT GGGTCTCTCT 420 ATTTCCTCTC CCTGGGTCTC TGTCTCCCTC CTTAAGTCTC TGCCTCTTGT CTCTCACCCA 480 TCTCTTGGTG TCTCTGCACT CTCTGTGCTA GGCGCCCCCC CATTTCCCTG GAATGCTGCC 540 CCTCTGGTTC TTCCACCCCG GAGGGGGAGG GGCTAGACTT TCTCCCCATT TCAAGCCCCC 600 CTGCCCCCCA GTGCACGGCC CCTGAGTTGG AGCAGGTTGG GGGTGGGGAG CGCTACCTGC 660 CTGAGCTGTG AAATGGGAGA GGGAGGCTGC CCCAGCCTGG GGGTTGTCTG GATCTCCCTG 720 AGGGGCCACA GGGCAGGGCC GGGAGGCTGG ATTAGGTTGA GGAAGGCTCC ACTTTTGAAG 780 GAACAGGGGC AGGGATCCAG AGCGATCTGG TGTCGGATCT GGCCTGAGAA GCAGGGAAGT 840 GCACTGGGGT GAGAGGCGTA GAAAAGGATG TGGGGTGGTG GTTCCAGGCG GGTGCTCATG 900 GGGAGGAATC TGCTGAGAAG GGAAGATCTG GTGGGGAATC CTTTGGGAGG CTTCGGGGAT 960 CTGAGGGATC CAGAAGAGAG TTCTGACAGG CTATCTAAGG AAATTTCTGT GCTTAGCTCC 1020 TTATTAACTC TTGCTTCAGG GAGCATGAAA ATCCCTGTTT TTTTACTGAT TATATGAATG 1080 AGCCTAGGGC TTCAAGAAGG AGCAGGTGTA ACTCCCCAAG TACAACCCCC TACATTCTCA 1140 GCCCCAGGCA CAGGCCACAC TTTCTCGTAC CCTCTTGCCT TCATTTCCAC ACTCAGCTCA 1200 CCCCCTCCAC CCCCACACAC ACTCCCTATT CAGCTGCTTT CTTGCCCCCT CTCGCATACC 1260 TGGGCCCGCA TGCCGGCCAG GGCTCAAGAA ATCTGTGCCT GCACACTCTC GCAGCATACC 1320 TGTGCACATG CACAGTCATC CTTGTGTATT TTTGTATATG CACTTTCTTG CACATTTTAC 1380 TTGCTCAGTC TCTTATTTGA AATGTCTTTA TAGTGTTTTT TTTAGTTTCC TTTATAGTTT 1440 CCTTTTCCAG CTGCTCTTCC TCTTCCCTCT TTCTTTCCTT TAACAAGAAA ATTGTTTTAA 1500 CATAATTCCT TCCTTCCTTC CTCCCTTTCT TCCTTCTTCT TGCAACTACT GATACCTCCC 1560 CTTTATCCAG CTTTGTGTGC CCTGGGCGGG TTGGCTTGGT GTACAAGGCT GCCAAGAGAG 1620 GAGGGGGTGG TTGGGTGTTG GTGAAGGAAT TTGGCGGGGC AGAGTTAGAC TGCAGCAAAC 1680 GGAAACTAGC TACACATCTT TTACTGGGAA GTGTATGGAT ACGCAGCAAA ATACTAGCCC 1740 TGGCAGTTTG GGCACAGTCC ACCCTTTTTT CCATCAGCCT GAACTATGGG AGTCTAGCTT 1800 TGAGGGTCCT CCCTGGGGGC GGGGAGGAGG GGACCCAGAC CTCCTGCAGT AGAGGGGTTG 1860 TGATACACAC CACGGCTCCT CCACTTTCCA GCTTCAGGCC TCAAAGAGGC CCCTTTCTCC 1920 CTGAGTCTCA ATTTCACTCC CTGTAAAATG GGGTAGCTAA TCCAACCCGG ACTGGGTCCC 1980 AGGGCTGTTG TAAGAATCCA AGGGAACTGT GTGGCAGTGC ATCGTCAGCA GTGGCAGTCA 2040 CTTCCCTTGT GACTGACACT GCTGTGTGCT TGGTTCCAGC TTGCAGTCAG GGCCCTACCC 2100 TCGAGAAGCT CGTGGTCCTT GGGGGAGCAG GTTGCACCAT GGGATTGCAA AAGCAATTCA 2160 GTTACCTGTC ATTGATTGCT GACTGTGTGC CAGACCCCGG GGTAGGCGCT TTCGGCCCCG 2220 GCTGCCTTTC TTCCTTTGGG ACTAACAGCT ATGTAGAAGA GGCAGCCCAC CCCTAAGGTT 2280 CAGGCATCTG CTCAACTAAA GCAGCTGCGG TTCTGAGTTG GGTTAGAACA TTGCAAGAGT 2340 TCATCAAGAG ACGGGGGAGA GTTCGGAGGT CAGGGTGAGG TGAGTCCCAG AGGAGACCAA 2400 GAAGAAGTGA TGTGAACTAG GTTTGGAGGG ATGAGTAGGA GTTTGAAGAA GAGAGAAAGG 2460 ACTTGAGATA GATAAAAACC AGTATGAATA AAGACTGGGA GGTGTTGTCA CTTGTGAAGT 2520
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